NDC 70518-4733
Doxepin Hydrochloride 150 mg capsule
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Leading Pharma, LLC's NDC 69315-163.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| LIFEPharma FZE | Dubai, United Arab Emirates | Makes it | Problems found, fixed voluntarilyNov 24, 2022 · 1 inspection |
Product details
- Generic drug
- Doxepin: every company that makes it
- Form
- capsule, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA211618
- On the market since
- Aug 24, 2026
- Package NDCs
70518-4733-0- Official label
- DailyMed (National Library of Medicine), updated Aug 24, 2026
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